Variant report
Variant | rs2597975 |
---|---|
Chromosome Location | chr12:11252797-11252798 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr12:11237724..11239418-chr12:11252570..11254241,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1031391 | 0.80[AFR][1000 genomes] |
rs1047710 | 0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1047711 | 0.84[AFR][1000 genomes] |
rs1047713 | 0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs10732561 | 0.80[ASN][1000 genomes] |
rs10734843 | 0.80[ASN][1000 genomes] |
rs10772398 | 0.80[ASN][1000 genomes] |
rs1376249 | 0.80[ASN][1000 genomes] |
rs1427754 | 0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1463237 | 0.80[ASN][1000 genomes] |
rs1650016 | 0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1650019 | 1.00[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.99[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1650021 | 0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1650022 | 0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1650023 | 0.89[AFR][1000 genomes];0.87[AMR][1000 genomes] |
rs1650024 | 0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs1650025 | 0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1650026 | 0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1650027 | 0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1650028 | 0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1650032 | 0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1650033 | 1.00[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1650034 | 0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1650035 | 0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1669406 | 0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1669407 | 0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1669409 | 0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1669413 | 0.89[AFR][1000 genomes];0.83[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs1669415 | 0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1669416 | 0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1669417 | 0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1669419 | 0.89[AFR][1000 genomes];0.83[AMR][1000 genomes] |
rs1669420 | 0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.80[ASN][1000 genomes] |
rs1669421 | 0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1669424 | 1.00[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.99[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1669425 | 0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1669426 | 0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1669430 | 1.00[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1669431 | 0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1669432 | 0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1669433 | 0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1669434 | 0.83[AFR][1000 genomes];0.82[AMR][1000 genomes] |
rs1669435 | 0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1669436 | 0.86[AFR][1000 genomes];0.85[AMR][1000 genomes] |
rs1817043 | 0.80[ASN][1000 genomes] |
rs1839569 | 0.80[ASN][1000 genomes] |
rs187328 | 1.00[ASW][hapmap];0.92[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];0.88[MEX][hapmap];1.00[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs2110097 | 0.92[CEU][hapmap] |
rs2255418 | 0.80[ASN][1000 genomes] |
rs2257110 | 0.80[ASN][1000 genomes] |
rs2264229 | 0.80[AFR][1000 genomes] |
rs2443094 | 0.80[AFR][1000 genomes] |
rs2443739 | 0.80[AFR][1000 genomes] |
rs2597934 | 0.80[AFR][1000 genomes] |
rs2597935 | 0.80[AFR][1000 genomes] |
rs2597939 | 0.80[AFR][1000 genomes] |
rs2597940 | 0.80[AFR][1000 genomes] |
rs2597943 | 0.80[AFR][1000 genomes] |
rs2597944 | 0.80[AFR][1000 genomes] |
rs2597945 | 0.80[AFR][1000 genomes] |
rs2597947 | 0.80[AFR][1000 genomes] |
rs2597949 | 0.80[AFR][1000 genomes] |
rs2597950 | 0.80[AFR][1000 genomes] |
rs2597951 | 0.80[AFR][1000 genomes] |
rs2597952 | 0.80[AFR][1000 genomes] |
rs2597953 | 1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2597955 | 0.80[AFR][1000 genomes] |
rs2597957 | 0.80[AFR][1000 genomes] |
rs2597959 | 0.80[AFR][1000 genomes] |
rs2597960 | 0.80[AFR][1000 genomes] |
rs2597963 | 0.80[AFR][1000 genomes] |
rs2597965 | 0.80[AFR][1000 genomes] |
rs2597966 | 0.80[AFR][1000 genomes] |
rs2597967 | 0.80[AFR][1000 genomes] |
rs2597968 | 0.80[AFR][1000 genomes] |
rs2597969 | 0.80[AFR][1000 genomes] |
rs2597970 | 0.80[AFR][1000 genomes] |
rs2597971 | 0.80[AFR][1000 genomes] |
rs2597972 | 0.80[AFR][1000 genomes] |
rs2597974 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2597984 | 0.80[ASN][1000 genomes] |
rs2597988 | 0.80[ASN][1000 genomes] |
rs2597990 | 0.80[ASN][1000 genomes] |
rs2599399 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2599400 | 0.81[AFR][1000 genomes] |
rs2599405 | 0.80[AFR][1000 genomes] |
rs2599411 | 0.80[AFR][1000 genomes] |
rs2599415 | 0.80[ASN][1000 genomes] |
rs2600332 | 0.80[AFR][1000 genomes] |
rs2600333 | 0.80[AFR][1000 genomes] |
rs2600334 | 0.80[AFR][1000 genomes] |
rs2600335 | 0.80[AFR][1000 genomes] |
rs2600336 | 0.80[AFR][1000 genomes] |
rs2600337 | 0.88[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs2600338 | 0.80[AFR][1000 genomes] |
rs2600339 | 0.80[AFR][1000 genomes] |
rs2600340 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2600341 | 0.80[AFR][1000 genomes] |
rs2600344 | 0.80[AFR][1000 genomes] |
rs2600345 | 0.80[AFR][1000 genomes] |
rs2600347 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2600366 | 0.80[AFR][1000 genomes] |
rs2600368 | 0.80[AFR][1000 genomes] |
rs2600369 | 0.80[AFR][1000 genomes] |
rs2600371 | 0.80[AFR][1000 genomes] |
rs2600372 | 0.80[AFR][1000 genomes] |
rs2600373 | 0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs2708323 | 0.80[ASN][1000 genomes] |
rs2708333 | 0.80[AFR][1000 genomes] |
rs2708334 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2708335 | 0.80[AFR][1000 genomes] |
rs2708336 | 0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2708340 | 0.81[AFR][1000 genomes] |
rs2708347 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2708351 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2708353 | 0.80[AFR][1000 genomes] |
rs2708354 | 0.80[AFR][1000 genomes] |
rs2708356 | 0.80[AFR][1000 genomes] |
rs2708357 | 0.80[AFR][1000 genomes] |
rs2708358 | 0.80[AFR][1000 genomes] |
rs2708359 | 0.80[AFR][1000 genomes] |
rs2708361 | 0.80[AFR][1000 genomes] |
rs2708362 | 0.80[AFR][1000 genomes] |
rs2708363 | 0.80[AFR][1000 genomes] |
rs2708364 | 0.80[AFR][1000 genomes] |
rs2708365 | 0.80[AFR][1000 genomes] |
rs2708366 | 0.80[AFR][1000 genomes] |
rs2900127 | 0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs2900577 | 0.80[ASN][1000 genomes] |
rs2923235 | 0.80[AFR][1000 genomes] |
rs319266 | 0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs319269 | 1.00[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs319270 | 0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs319276 | 1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes] |
rs319277 | 0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs34692077 | 0.95[AFR][1000 genomes] |
rs35318883 | 0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs35672518 | 0.86[ASN][1000 genomes] |
rs35762060 | 0.83[ASN][1000 genomes] |
rs36147394 | 0.80[AFR][1000 genomes] |
rs36185691 | 0.80[AFR][1000 genomes] |
rs3911150 | 0.92[CEU][hapmap];0.96[GIH][hapmap];0.91[TSI][hapmap] |
rs4388985 | 0.80[ASN][1000 genomes] |
rs4763632 | 0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs4763636 | 0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.80[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs4763637 | 0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs61928567 | 0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs61928603 | 0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.90[ASN][1000 genomes] |
rs61928604 | 0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs61928606 | 0.85[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs61928608 | 0.83[AFR][1000 genomes] |
rs61928609 | 0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs61928614 | 0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs61928615 | 0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs61928650 | 0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs61931269 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs61931280 | 0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs6488353 | 0.87[AFR][1000 genomes] |
rs68045377 | 0.81[EUR][1000 genomes] |
rs68071847 | 0.95[ASN][1000 genomes] |
rs7296270 | 0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs7298947 | 0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs7304814 | 0.86[ASN][1000 genomes] |
rs73051387 | 0.81[EUR][1000 genomes] |
rs73053413 | 0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs7306087 | 0.80[ASN][1000 genomes] |
rs73066828 | 0.93[EUR][1000 genomes] |
rs73066852 | 0.93[EUR][1000 genomes] |
rs7315843 | 0.80[ASN][1000 genomes] |
rs7487324 | 0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs7962445 | 0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs7973298 | 0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs7978274 | 1.00[CHB][hapmap] |
rs8181 | 0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs977474 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes] |
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2758294 | chr12:10969620-11714921 | Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 52 gene(s) | inside rSNPs | diseases |
2 | esv2759879 | chr12:10969620-11714921 | Genic enhancers Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 52 gene(s) | inside rSNPs | diseases |
3 | nsv1038277 | chr12:11060978-11504091 | Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 40 gene(s) | inside rSNPs | diseases |
4 | nsv428272 | chr12:11069845-11714921 | Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 47 gene(s) | inside rSNPs | diseases |
5 | esv3503763 | chr12:11161162-11275828 | Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
6 | esv3503774 | chr12:11161325-11275786 | Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
7 | nsv1038709 | chr12:11165117-11283834 | Enhancers Strong transcription ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
8 | esv1804289 | chr12:11166879-11294110 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
9 | nsv8917 | chr12:11168232-11293747 | Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
10 | esv1827548 | chr12:11168557-11277324 | Weak transcription ZNF genes & repeats Strong transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
11 | esv2760999 | chr12:11170837-11276036 | ZNF genes & repeats Strong transcription Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
12 | esv1835477 | chr12:11174302-11298269 | Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
13 | nsv898782 | chr12:11185236-11283763 | Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
14 | nsv898783 | chr12:11185236-11338781 | ZNF genes & repeats Genic enhancers Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 26 gene(s) | inside rSNPs | diseases |
15 | nsv898784 | chr12:11188140-11341521 | Active TSS ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 25 gene(s) | inside rSNPs | diseases |
16 | esv3503785 | chr12:11190186-11291382 | ZNF genes & repeats Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
17 | esv3503796 | chr12:11190186-11291382 | Strong transcription ZNF genes & repeats Weak transcription Genic enhancers Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
18 | esv1848930 | chr12:11190763-11258011 | Weak transcription ZNF genes & repeats Strong transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
19 | nsv1050050 | chr12:11192046-11436359 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 31 gene(s) | inside rSNPs | diseases |
20 | nsv1046400 | chr12:11195634-11256817 | Strong transcription ZNF genes & repeats Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
21 | esv3408962 | chr12:11195947-11269922 | ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
22 | nsv1053783 | chr12:11203509-11495584 | Weak transcription ZNF genes & repeats Genic enhancers Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 32 gene(s) | inside rSNPs | diseases |
23 | esv1818975 | chr12:11203777-11257793 | Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
24 | esv5827 | chr12:11204250-11275862 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
25 | esv3389516 | chr12:11207203-11290088 | Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
26 | esv3335920 | chr12:11207222-11278359 | ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
27 | esv3503829 | chr12:11207236-11278424 | Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
28 | esv3503841 | chr12:11207236-11278424 | Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
29 | esv6373 | chr12:11209985-11282106 | Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
30 | esv3350574 | chr12:11212837-11284853 | Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
31 | esv1805438 | chr12:11213879-11257793 | Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
32 | esv1807067 | chr12:11214215-11568895 | Flanking Active TSS Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 33 gene(s) | inside rSNPs | diseases |
33 | esv1816499 | chr12:11215094-11257793 | Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
34 | esv1831521 | chr12:11215094-11257793 | ZNF genes & repeats Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
35 | esv1826511 | chr12:11215912-11256408 | Strong transcription Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
36 | esv1819869 | chr12:11215912-11257793 | Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
37 | esv1805584 | chr12:11218198-11256608 | ZNF genes & repeats Bivalent Enhancer Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
38 | esv8675 | chr12:11218264-11290113 | Weak transcription ZNF genes & repeats Strong transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
39 | esv1803074 | chr12:11218398-11256408 | Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
40 | esv1803107 | chr12:11218398-11256408 | Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
41 | esv1830081 | chr12:11218657-11256608 | Strong transcription ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
42 | esv1797695 | chr12:11219033-11256608 | Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
43 | esv1834356 | chr12:11220712-11261335 | ZNF genes & repeats Enhancers Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
44 | nsv1046393 | chr12:11220712-11274426 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
45 | nsv1038879 | chr12:11220712-11280303 | Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
46 | nsv1042134 | chr12:11220712-11328131 | Enhancers Strong transcription ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 21 gene(s) | inside rSNPs | diseases |
47 | nsv1043344 | chr12:11220827-11308162 | ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
48 | esv3432628 | chr12:11220915-11257282 | Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
49 | esv3491948 | chr12:11232746-11275708 | ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
50 | esv3491949 | chr12:11232746-11275708 | Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
SNP | Gene | Cis/trans | Tissue | Source |
---|---|---|---|---|
rs2597975 | GABARAPL1 | cis | lymphoblastoid | seeQTL |
rs2597975 | TAS2R46 | cis | cerebellum | SCAN |
rs2597975 | PRR4 | cis | lymphoblastoid | seeQTL |
rs2597975 | TAS2R19 | cis | cerebellum | SCAN |
rs2597975 | PRH1 | cis | cerebellum | SCAN |
rs2597975 | AICDA | cis | parietal | SCAN |
rs2597975 | TAS2R19 | cis | parietal | SCAN |
rs2597975 | TAS2R43 | cis | cerebellum | SCAN |
rs2597975 | TAS2R20 | cis | cerebellum | SCAN |
rs2597975 | CLEC1B | cis | parietal | SCAN |
rs2597975 | TAS2R13 | cis | cerebellum | SCAN |
rs2597975 | TAS2R14 | cis | lung | GTEx |
rs2597975 | TAS2R14 | cis | Thyroid | GTEx |
rs2597975 | TAS2R15 | cis | Muscle Skeletal | GTEx |
rs2597975 | TAS2R14 | cis | parietal | SCAN |
rs2597975 | TAS2R14 | cis | cerebellum | SCAN |
rs2597975 | TAS2R15 | cis | Thyroid | GTEx |
rs2597975 | TAS2R31 | cis | parietal | SCAN |
rs2597975 | TAS2R20 | cis | lung | GTEx |
rs2597975 | TAS2R20 | cis | Skin Sun Exposed Lower leg | GTEx |
rs2597975 | TAS2R50 | cis | parietal | SCAN |
rs2597975 | PRR4 | cis | cerebellum | SCAN |
rs2597975 | TAS2R31 | cis | cerebellum | SCAN |
rs2597975 | TAS2R14 | cis | Artery Tibial | GTEx |
rs2597975 | TAS2R50 | cis | cerebellum | SCAN |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:11203800-11261200 | Weak transcription | Primary Natural Killer cells fromperipheralblood | blood |
2 | chr12:11205800-11269200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
3 | chr12:11208600-11259600 | Weak transcription | hESC Derived CD56+ Mesoderm Cultured Cells | ES cell derived |
4 | chr12:11218200-11256800 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
5 | chr12:11221200-11259600 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
6 | chr12:11225200-11261000 | Weak transcription | Fetal Stomach | stomach |
7 | chr12:11234400-11261200 | Weak transcription | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
8 | chr12:11234400-11261400 | Weak transcription | Primary T cells fromperipheralblood | blood |
9 | chr12:11237200-11256400 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
10 | chr12:11237200-11262200 | Weak transcription | Duodenum Smooth Muscle | Duodenum |
11 | chr12:11239200-11283600 | Weak transcription | Fetal Thymus | thymus |
12 | chr12:11239600-11261600 | Weak transcription | Primary T helper naive cells fromperipheralblood | blood |
13 | chr12:11239800-11261400 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
14 | chr12:11240200-11253800 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
15 | chr12:11241800-11259400 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
16 | chr12:11242000-11257200 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
17 | chr12:11244800-11261400 | Weak transcription | Primary B cells from peripheral blood | blood |
18 | chr12:11245200-11286000 | Weak transcription | Ovary | ovary |
19 | chr12:11249400-11255600 | Weak transcription | Primary T helper cells fromperipheralblood | blood |
20 | chr12:11249600-11261600 | Weak transcription | Primary T killer naive cells fromperipheralblood | blood |
21 | chr12:11249800-11253800 | Weak transcription | Fetal Intestine Large | intestine |
22 | chr12:11249800-11261600 | Weak transcription | Primary T regulatory cells fromperipheralblood | blood |
23 | chr12:11250600-11255600 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
24 | chr12:11250800-11254000 | ZNF genes & repeats | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
25 | chr12:11251000-11256600 | Weak transcription | Fetal Lung | lung |
26 | chr12:11251000-11276200 | Weak transcription | iPS-18 Cell Line | embryonic stem cell |
27 | chr12:11251200-11259600 | Weak transcription | Thymus | Thymus |
28 | chr12:11251200-11269800 | Weak transcription | H1 Cell Line | embryonic stem cell |
29 | chr12:11251400-11259200 | Weak transcription | Primary B cells from cord blood | blood |
30 | chr12:11251400-11259600 | Weak transcription | Monocytes-CD14+_RO01746 | blood |
31 | chr12:11251400-11260000 | Weak transcription | A549 | lung |
32 | chr12:11251800-11263200 | Weak transcription | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
33 | chr12:11252000-11255400 | Weak transcription | Primary T helper naive cells from peripheral blood | blood |
34 | chr12:11252000-11261400 | Weak transcription | Left Ventricle | heart |
35 | chr12:11252200-11252800 | ZNF genes & repeats | Primary hematopoietic stem cells | blood |
36 | chr12:11252200-11258800 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
37 | chr12:11252200-11274800 | Weak transcription | HSMM | muscle |
38 | chr12:11252400-11259600 | Weak transcription | Primary monocytes fromperipheralblood | blood |
39 | chr12:11252400-11261400 | Weak transcription | Psoas Muscle | Psoas |
40 | chr12:11252600-11261200 | Weak transcription | Primary T helper memory cells from peripheral blood 2 | blood |